Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond
- Autores
- Lira, María Cecilia; Rosa, Francisco Damián; Baldi, M. E.; Soares Machado, Mileni; Palma, Alejandra Graciela; Marino, Gabriela Inés; Costas, Monica Alejandra; Rubio, Maria Fernanda
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Adipocytes are considered to be critical in the tumoral microenvironment of breast cancer. However, most studies have focused on linking obesity and cancer, ignoring changes on normal adipocytes. Therefore, we retrieved microarray data from a GEO dataset (GSE95827) to analyse transcriptional changes in 3T3-L1 adipocytes after 3 days of co-culture with MCF7 (Ad+MCF) or MDAMB-231 breast cancer cell (Ad+MDA).By GEO2R tool, we determined 245 up-regulated genes in Ad+MCF7 and 215 in Ad+MDA compared to adipocytes alone (p<0.01), but only 68 of them overlapped between conditions. Gene OntologyAnalysis was performed and showed that the biological process enrichment is completely different between MDA-MB-231 and MCF7-co-cultured adipocytes. Even more, co-culture with MDA-MB-231cells enriched adipocytes with genes involved in Cellular response to interleukin-6 (GO:0071354) and Positive regulation of NIK/NF-kB signaling (GO:1901224), both related to inflammation. Transcription factors (TF) analysis by ISMARA platform predicted that NF-kB family members had the highest activity in Ad+MDA. To verify this result, we performed immunofluorescence assays detecting the presence of phosphorylated NF-kB subunit p65. MDA-MB-231 cells significantly led to a higher fluorescence intensity in adipocyte nuclei than MCF7 did when compared to basal condition. Moreover, mRNA levels of NF-kB targets as cxcl1, cxcl5, il6 obtained from the analyseddataset were found up-regulated in Ad+MDA respect to adipocytes alone (p<0.05). Interestingly, expression levels of Il6 family members (Il6 and Il11) were up-regulated in MDA-MB-231 cell line compared to MCF7 cells in three different public datasets, which could explain NF-kB activation only in Ad+MDA.These results suggest that breast cancer cells stimulate adjacent adipocytes in different ways leading or not to inflammation in adipocytes.
Fil: Lira, María Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Rosa, Francisco Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Baldi, M. E.. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Soares Machado, Mileni. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Palma, Alejandra Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Marino, Gabriela Inés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Costas, Monica Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Rubio, Maria Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
LXIII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXVIII Reunión Anual de la Sociedad Argentina de Inmunología y Reunión Anual de la Sociedad Argentina de Fisiología
Argentina
Sociedad Argentina de Investigación Clínica
Sociedad Argentina de Inmunología
Sociedad Argentina de Fisiología - Materia
-
ADIPOCYTES
BREAST CANCER
MICROENVIRONMENT - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/269344
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Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respondLira, María CeciliaRosa, Francisco DamiánBaldi, M. E.Soares Machado, MileniPalma, Alejandra GracielaMarino, Gabriela InésCostas, Monica AlejandraRubio, Maria FernandaADIPOCYTESBREAST CANCERMICROENVIRONMENThttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Adipocytes are considered to be critical in the tumoral microenvironment of breast cancer. However, most studies have focused on linking obesity and cancer, ignoring changes on normal adipocytes. Therefore, we retrieved microarray data from a GEO dataset (GSE95827) to analyse transcriptional changes in 3T3-L1 adipocytes after 3 days of co-culture with MCF7 (Ad+MCF) or MDAMB-231 breast cancer cell (Ad+MDA).By GEO2R tool, we determined 245 up-regulated genes in Ad+MCF7 and 215 in Ad+MDA compared to adipocytes alone (p<0.01), but only 68 of them overlapped between conditions. Gene OntologyAnalysis was performed and showed that the biological process enrichment is completely different between MDA-MB-231 and MCF7-co-cultured adipocytes. Even more, co-culture with MDA-MB-231cells enriched adipocytes with genes involved in Cellular response to interleukin-6 (GO:0071354) and Positive regulation of NIK/NF-kB signaling (GO:1901224), both related to inflammation. Transcription factors (TF) analysis by ISMARA platform predicted that NF-kB family members had the highest activity in Ad+MDA. To verify this result, we performed immunofluorescence assays detecting the presence of phosphorylated NF-kB subunit p65. MDA-MB-231 cells significantly led to a higher fluorescence intensity in adipocyte nuclei than MCF7 did when compared to basal condition. Moreover, mRNA levels of NF-kB targets as cxcl1, cxcl5, il6 obtained from the analyseddataset were found up-regulated in Ad+MDA respect to adipocytes alone (p<0.05). Interestingly, expression levels of Il6 family members (Il6 and Il11) were up-regulated in MDA-MB-231 cell line compared to MCF7 cells in three different public datasets, which could explain NF-kB activation only in Ad+MDA.These results suggest that breast cancer cells stimulate adjacent adipocytes in different ways leading or not to inflammation in adipocytes.Fil: Lira, María Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Rosa, Francisco Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Baldi, M. E.. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Soares Machado, Mileni. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Palma, Alejandra Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Marino, Gabriela Inés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Costas, Monica Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Rubio, Maria Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaLXIII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXVIII Reunión Anual de la Sociedad Argentina de Inmunología y Reunión Anual de la Sociedad Argentina de FisiologíaArgentinaSociedad Argentina de Investigación ClínicaSociedad Argentina de InmunologíaSociedad Argentina de FisiologíaFundación Revista Medicina2020info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/269344Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond; LXIII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXVIII Reunión Anual de la Sociedad Argentina de Inmunología y Reunión Anual de la Sociedad Argentina de Fisiología; Argentina; 2020; 117-1170025-76801669-9106CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.medicinabuenosaires.com/indices-de-2020/Nacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:03:22Zoai:ri.conicet.gov.ar:11336/269344instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:03:23.22CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond |
title |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond |
spellingShingle |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond Lira, María Cecilia ADIPOCYTES BREAST CANCER MICROENVIRONMENT |
title_short |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond |
title_full |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond |
title_fullStr |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond |
title_full_unstemmed |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond |
title_sort |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond |
dc.creator.none.fl_str_mv |
Lira, María Cecilia Rosa, Francisco Damián Baldi, M. E. Soares Machado, Mileni Palma, Alejandra Graciela Marino, Gabriela Inés Costas, Monica Alejandra Rubio, Maria Fernanda |
author |
Lira, María Cecilia |
author_facet |
Lira, María Cecilia Rosa, Francisco Damián Baldi, M. E. Soares Machado, Mileni Palma, Alejandra Graciela Marino, Gabriela Inés Costas, Monica Alejandra Rubio, Maria Fernanda |
author_role |
author |
author2 |
Rosa, Francisco Damián Baldi, M. E. Soares Machado, Mileni Palma, Alejandra Graciela Marino, Gabriela Inés Costas, Monica Alejandra Rubio, Maria Fernanda |
author2_role |
author author author author author author author |
dc.subject.none.fl_str_mv |
ADIPOCYTES BREAST CANCER MICROENVIRONMENT |
topic |
ADIPOCYTES BREAST CANCER MICROENVIRONMENT |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Adipocytes are considered to be critical in the tumoral microenvironment of breast cancer. However, most studies have focused on linking obesity and cancer, ignoring changes on normal adipocytes. Therefore, we retrieved microarray data from a GEO dataset (GSE95827) to analyse transcriptional changes in 3T3-L1 adipocytes after 3 days of co-culture with MCF7 (Ad+MCF) or MDAMB-231 breast cancer cell (Ad+MDA).By GEO2R tool, we determined 245 up-regulated genes in Ad+MCF7 and 215 in Ad+MDA compared to adipocytes alone (p<0.01), but only 68 of them overlapped between conditions. Gene OntologyAnalysis was performed and showed that the biological process enrichment is completely different between MDA-MB-231 and MCF7-co-cultured adipocytes. Even more, co-culture with MDA-MB-231cells enriched adipocytes with genes involved in Cellular response to interleukin-6 (GO:0071354) and Positive regulation of NIK/NF-kB signaling (GO:1901224), both related to inflammation. Transcription factors (TF) analysis by ISMARA platform predicted that NF-kB family members had the highest activity in Ad+MDA. To verify this result, we performed immunofluorescence assays detecting the presence of phosphorylated NF-kB subunit p65. MDA-MB-231 cells significantly led to a higher fluorescence intensity in adipocyte nuclei than MCF7 did when compared to basal condition. Moreover, mRNA levels of NF-kB targets as cxcl1, cxcl5, il6 obtained from the analyseddataset were found up-regulated in Ad+MDA respect to adipocytes alone (p<0.05). Interestingly, expression levels of Il6 family members (Il6 and Il11) were up-regulated in MDA-MB-231 cell line compared to MCF7 cells in three different public datasets, which could explain NF-kB activation only in Ad+MDA.These results suggest that breast cancer cells stimulate adjacent adipocytes in different ways leading or not to inflammation in adipocytes. Fil: Lira, María Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Rosa, Francisco Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Baldi, M. E.. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Soares Machado, Mileni. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Palma, Alejandra Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Marino, Gabriela Inés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Costas, Monica Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Rubio, Maria Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina LXIII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXVIII Reunión Anual de la Sociedad Argentina de Inmunología y Reunión Anual de la Sociedad Argentina de Fisiología Argentina Sociedad Argentina de Investigación Clínica Sociedad Argentina de Inmunología Sociedad Argentina de Fisiología |
description |
Adipocytes are considered to be critical in the tumoral microenvironment of breast cancer. However, most studies have focused on linking obesity and cancer, ignoring changes on normal adipocytes. Therefore, we retrieved microarray data from a GEO dataset (GSE95827) to analyse transcriptional changes in 3T3-L1 adipocytes after 3 days of co-culture with MCF7 (Ad+MCF) or MDAMB-231 breast cancer cell (Ad+MDA).By GEO2R tool, we determined 245 up-regulated genes in Ad+MCF7 and 215 in Ad+MDA compared to adipocytes alone (p<0.01), but only 68 of them overlapped between conditions. Gene OntologyAnalysis was performed and showed that the biological process enrichment is completely different between MDA-MB-231 and MCF7-co-cultured adipocytes. Even more, co-culture with MDA-MB-231cells enriched adipocytes with genes involved in Cellular response to interleukin-6 (GO:0071354) and Positive regulation of NIK/NF-kB signaling (GO:1901224), both related to inflammation. Transcription factors (TF) analysis by ISMARA platform predicted that NF-kB family members had the highest activity in Ad+MDA. To verify this result, we performed immunofluorescence assays detecting the presence of phosphorylated NF-kB subunit p65. MDA-MB-231 cells significantly led to a higher fluorescence intensity in adipocyte nuclei than MCF7 did when compared to basal condition. Moreover, mRNA levels of NF-kB targets as cxcl1, cxcl5, il6 obtained from the analyseddataset were found up-regulated in Ad+MDA respect to adipocytes alone (p<0.05). Interestingly, expression levels of Il6 family members (Il6 and Il11) were up-regulated in MDA-MB-231 cell line compared to MCF7 cells in three different public datasets, which could explain NF-kB activation only in Ad+MDA.These results suggest that breast cancer cells stimulate adjacent adipocytes in different ways leading or not to inflammation in adipocytes. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Reunión Journal http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
status_str |
publishedVersion |
format |
conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/269344 Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond; LXIII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXVIII Reunión Anual de la Sociedad Argentina de Inmunología y Reunión Anual de la Sociedad Argentina de Fisiología; Argentina; 2020; 117-117 0025-7680 1669-9106 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/269344 |
identifier_str_mv |
Adipocytes in the breast cancer microenvironment: different tumor cells, different ways to respond; LXIII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXVIII Reunión Anual de la Sociedad Argentina de Inmunología y Reunión Anual de la Sociedad Argentina de Fisiología; Argentina; 2020; 117-117 0025-7680 1669-9106 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.medicinabuenosaires.com/indices-de-2020/ |
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openAccess |
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Nacional |
dc.publisher.none.fl_str_mv |
Fundación Revista Medicina |
publisher.none.fl_str_mv |
Fundación Revista Medicina |
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